Canonical Allele Identifier: CA057086

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 418929
• ClinVar RCV Id: RCV000484560 ; RCV000583734 ; RCV001035516
• dbSNP Id: rs151196169
• ExAC: 1:45795013 T / C
• gnomAD v2: 1-45795013-T-C
• gnomAD v3: 1-45329341-T-C
• gnomAD v4: 1-45329341-T-C
• MyVariant Identifiers: chr1:g.45795013T>C (hg19) ; chr1:g.45329341T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45329341T>C , CM000663.2:g.45329341T>C	GRCh38
NC_000001.10:g.45795013T>C , CM000663.1:g.45795013T>C	GRCh37
NC_000001.9:g.45567600T>C	NCBI36
NG_008189.1:g.16130A>G , LRG_220:g.16130A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.1147A>G	ENSP00000410263.2:p.Thr383Ala
ENST00000435155.2:c.1564A>G	ENSP00000403655.2:p.Thr522Ala
ENST00000467459.6:c.*393A>G	ENSP00000435889.2:n.*393A>G
ENST00000483127.2:c.1549A>G	ENSP00000436469.2:p.Thr517Ala
ENST00000485271.6:c.*274A>G	ENSP00000431264.2:n.*274A>G
ENST00000529892.6:c.1384A>G	ENSP00000432528.2:p.Thr462Ala
ENST00000533178.6:c.*860A>G	ENSP00000436430.2:n.*860A>G
ENST00000672314.2:c.1531A>G	ENSP00000500828.2:p.Thr511Ala
ENST00000710952.2:c.1615A>G MANE Plus Clinical	ENSP00000518552.2:p.Thr539Ala
ENST00000672818.3:c.1606A>G	ENSP00000500891.1:p.Thr536Ala
ENST00000456914.7:c.1531A>G MANE Select	ENSP00000407590.2:p.Thr511Ala
ENST00000671898.1:c.*274A>G	ENSP00000499896.1:n.*274A>G
ENST00000672011.1:c.*860A>G	ENSP00000500418.1:n.*860A>G
ENST00000672818.2:c.1606A>G	ENSP00000500891.1:p.Thr536Ala
ENST00000354383.10:c.1534A>G	ENSP00000346354.6:p.Thr512Ala
ENST00000355498.6:c.1531A>G	ENSP00000347685.2:p.Thr511Ala
ENST00000372098.7:c.1606A>G	ENSP00000361170.3:p.Thr536Ala
ENST00000372104.5:c.1531A>G	ENSP00000361176.1:p.Thr511Ala
ENST00000372110.7:c.1576A>G	ENSP00000361182.3:p.Thr526Ala
ENST00000372115.7:c.1573A>G	ENSP00000361187.3:p.Thr525Ala
ENST00000448481.5:c.1564A>G	ENSP00000409718.1:p.Thr522Ala
ENST00000450313.5:c.1615A>G	ENSP00000408176.1:p.Thr539Ala
ENST00000456914.6:c.1531A>G	ENSP00000407590.2:p.Thr511Ala
ENST00000467459.5:c.948A>G	ENSP00000435889.1:n.948A>G
ENST00000475516.5:c.*1344A>G	ENSP00000433843.1:n.*1344A>G
ENST00000481571.5:c.*1344A>G	ENSP00000436597.1:n.*1344A>G
ENST00000482094.5:n.852A>G
ENST00000485271.5:c.408A>G
ENST00000488731.6:c.616A>G	ENSP00000432330.1:p.Thr206Ala
ENST00000528013.6:c.1573A>G	ENSP00000433130.2:p.Thr525Ala
ENST00000529892.5:c.606A>G
ENST00000529984.5:c.616A>G	ENSP00000437093.1:p.Thr206Ala
ENST00000531105.5:c.*23A>G	ENSP00000431292.1:n.*23A>G
ENST00000533178.5:c.1160A>G	ENSP00000436430.1:n.1160A>G
NM_001048171.1:c.1573A>G	NP_001041636.1:p.Thr525Ala
NM_001048172.1:c.1534A>G	NP_001041637.1:p.Thr512Ala
NM_001048173.1:c.1531A>G	NP_001041638.1:p.Thr511Ala
NM_001048174.1:c.1531A>G	NP_001041639.1:p.Thr511Ala
NM_001128425.1:c.1615A>G , LRG_220t1:c.1615A>G	NP_001121897.1:p.Thr539Ala
NM_001293190.1:c.1576A>G	NP_001280119.1:p.Thr526Ala
NM_001293191.1:c.1564A>G	NP_001280120.1:p.Thr522Ala
NM_001293192.1:c.1255A>G	NP_001280121.1:p.Thr419Ala
NM_001293195.1:c.1531A>G	NP_001280124.1:p.Thr511Ala
NM_001293196.1:c.1255A>G	NP_001280125.1:p.Thr419Ala
NM_012222.2:c.1606A>G	NP_036354.1:p.Thr536Ala
XM_011541497.1:c.1591A>G	XP_011539799.1:p.Thr531Ala
XM_011541498.1:c.1573A>G	XP_011539800.1:p.Thr525Ala
XM_011541499.1:c.1573A>G	XP_011539801.1:p.Thr525Ala
XM_011541500.1:c.1573A>G	XP_011539802.1:p.Thr525Ala
XM_011541501.1:c.1573A>G	XP_011539803.1:p.Thr525Ala
XM_011541502.1:c.1573A>G	XP_011539804.1:p.Thr525Ala
XM_011541503.1:c.1573A>G	XP_011539805.1:p.Thr525Ala
XM_011541504.1:c.1564A>G	XP_011539806.1:p.Thr522Ala
XM_011541505.1:c.1153A>G	XP_011539807.1:p.Thr385Ala
XM_011541506.1:c.1153A>G	XP_011539808.1:p.Thr385Ala
XM_011541507.1:c.1144A>G	XP_011539809.1:p.Thr382Ala
XM_011541508.1:c.1159A>G	XP_011539810.1:p.Thr387Ala
XR_946658.1:n.1842A>G
NM_001350650.1:c.1186A>G	NP_001337579.1:p.Thr396Ala
NM_001350651.1:c.1186A>G	NP_001337580.1:p.Thr396Ala
NR_146882.1:n.1969A>G
NR_146883.1:n.1783A>G
XM_011541497.3:c.1591A>G	XP_011539799.1:p.Thr531Ala
XM_011541500.3:c.1573A>G	XP_011539802.1:p.Thr525Ala
XM_011541501.2:c.1573A>G	XP_011539803.1:p.Thr525Ala
XM_011541502.2:c.1573A>G	XP_011539804.1:p.Thr525Ala
XM_011541503.2:c.1573A>G	XP_011539805.1:p.Thr525Ala
XM_011541504.2:c.1564A>G	XP_011539806.1:p.Thr522Ala
XM_011541505.2:c.1153A>G	XP_011539807.1:p.Thr385Ala
XM_011541506.2:c.1153A>G	XP_011539808.1:p.Thr385Ala
XM_017001331.1:c.1573A>G	XP_016856820.1:p.Thr525Ala
XM_017001332.1:c.1573A>G	XP_016856821.1:p.Thr525Ala
XM_017001333.1:c.1573A>G	XP_016856822.1:p.Thr525Ala
XM_017001334.1:c.1534A>G	XP_016856823.1:p.Thr512Ala
XM_017001335.1:c.1255A>G	XP_016856824.1:p.Thr419Ala
XM_017001336.1:c.1186A>G	XP_016856825.1:p.Thr396Ala
XM_017001337.1:c.1186A>G	XP_016856826.1:p.Thr396Ala
XM_024447244.1:c.1186A>G	XP_024303012.1:p.Thr396Ala
XM_024447245.1:c.1186A>G	XP_024303013.1:p.Thr396Ala
XM_024447248.1:c.1144A>G	XP_024303016.1:p.Thr382Ala
XM_024447249.1:c.1015A>G	XP_024303017.1:p.Thr339Ala
XM_024447250.1:c.1015A>G	XP_024303018.1:p.Thr339Ala
XM_024447251.1:c.1015A>G	XP_024303019.1:p.Thr339Ala
XR_001737190.1:n.1756A>G
XR_001737192.1:n.1568A>G
XR_002956643.1:n.1748A>G
XR_002956644.1:n.2283A>G
XR_946658.2:n.1856A>G
NM_001048171.2:c.1531A>G	NP_001041636.2:p.Thr511Ala
NM_001128425.2:c.1615A>G MANE Plus Clinical	NP_001121897.1:p.Thr539Ala
NM_001048172.2:c.1534A>G	NP_001041637.1:p.Thr512Ala
NM_001048173.2:c.1531A>G	NP_001041638.1:p.Thr511Ala
NM_001048174.2:c.1531A>G MANE Select	NP_001041639.1:p.Thr511Ala
NM_001293190.2:c.1576A>G	NP_001280119.1:p.Thr526Ala
NM_001293191.2:c.1564A>G	NP_001280120.1:p.Thr522Ala
NM_001293192.2:c.1255A>G	NP_001280121.1:p.Thr419Ala
NM_001293195.2:c.1531A>G	NP_001280124.1:p.Thr511Ala
NM_001293196.2:c.1255A>G	NP_001280125.1:p.Thr419Ala
NM_001350650.2:c.1186A>G	NP_001337579.1:p.Thr396Ala
NM_001350651.2:c.1186A>G	NP_001337580.1:p.Thr396Ala
NM_012222.3:c.1606A>G	NP_036354.1:p.Thr536Ala
NR_146882.2:n.1939A>G
NR_146883.2:n.1788A>G